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|Articles|March 1, 2016

Can you prove it to the FDA?

Attend our upcoming webinar on February 11, 2016 to learn how to foster your relationships with contract partners to develop a quality surveillance program that will meet FDA scrutiny.

 

Are you Effectively Monitoring your Contract Lab?

Attend our upcoming webinar on March 23, 2016 to learn how to foster your relationships with contract partners to develop a quality surveillance program that will meet FDA scrutiny. Hear from two Eurofins Lancaster Laboratories’ Quality Assurance experts, as well as our guest presenter, Sue Schniepp with Regulatory Compliance Associates.

Click here to register for free!

 

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The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.